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V2O5 nanowires were doped with Ru4+ using a hydrothermal process. RuxV2−xO5 composites were characterized by x-ray diffraction, energy-dispersive x-ray analysis, scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HRTEM). The electrochemical performance of the RuxV2−xO5 nanowires/carbon composites were evaluated by cyclic voltammetry and galvanostatic charge-discharge techniques. The RuxV2−xO5/carbon exhibited a maximum specific capacitance of 351 F·g−1 at a scan rate of 5 mV/s in a symmetric coin cell device. The asymmetric hybrid supercapacitor device achieved a specific cell capacitance of 237 F·g−1 at a scan rate of 5 mV/s, which delivers a high energy and power of 74.8 Wh·kg−1 and 5994.5 W·kg−1, respectively.

The use of immiscible polymer blends in gas separations is limited due to uncontrollable phase separation. In contrast, compatibilized immiscible polymer blends can be used as precursors with controlled morphologies that allow for a unique pore architecture. Herein, an immiscible polymer blend (1:1) comprising polybenzimidazole (PBI) and the copolyimide 6FDA-DAM:DABA [3:2], derived from reacting 4,4-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) with 2,4,6-trimethyl-1,3-phenylenediamine (DAM) and 3,5-diaminobenzoic acid (DABA), were combined with durene diamine as a compatibilizer. The compatibilizer helped reduce the 6FDD domain sizes from 5.6 µm down to 0.77 µm and induced a more even 6FDA distribution and the formation of continuous thin-selective PBI layers. The carbon–carbon composite membranes derived from the compatibilized immiscible polymer blends showed a 3-fold increase in both H2 permeability and H2/CO2 selectivity compared to the membranes derived from non-compatibilized polymer blends. The H2 permeability of the compatibilized immiscible polymer blends increased from 3.6 to 27 Barrer, and their H2/CO2 selectivity increased from 7.2 to 20. The graphitic domain size of the carbon–carbon composite membranes derived from the polymer blends also increased from 6.3 nm for the non-compatibilized blend to 10.0 nm for the compatibilized blend.

Carbon molecular sieve membranes (CMSMs) were prepared by carbonizing the high free volume polyimide BTDA-BAF that is obtained from the reaction of benzophenone-3,3′,4,4′-tetracarboxylic dianhydride (BTDA) and 9,9-bis(4-aminophenyl) fluorene (BAF). The bulky cardo groups prevented a tight packing and rotation of the chains that leads to high permeabilities of their CMSMs. The incorporation of metal–organic polyhedra 18 (MOP-18, a copper-based MOP) in the BTDA-BAF polymer before pyrolysis at 550 °C prevented the collapse of the pores and the aging of the CMSMs. It was found that upon decomposition of MOP-18, a distribution of copper nanoparticles minimized the collapse of the graphitic sheets that formed the micropores and mesopores in the CMSM. The pillared CMSMs displayed CO2 and CH4 permeabilities of 12,729 and 659 Barrer, respectively, with a CO2/CH4 selectivity of 19.3 after 3 weeks of aging. The permselectivity properties of these membranes was determined to be at the 2019 Robeson upper bound. In contrast, the CMSMs from pure BTDA-BAF aged three times faster than the CMSMs from MOP-18/BTDA-BAF and exhibited lower CO2 and CH4 permeabilities of 5337 and 573 Barrer, respectively, with a CO2/CH4 selectivity of 9.3. The non-pillared CMSMs performed below the upper bound.

An acrylonitrile based copolymer, poly(acrylonitrile-co-itaconic acid), P(AN-co-IA) was synthesized with different amounts of itaconic acid (IA) to study in situ porogen activity of IA to produce porous carbon nanofibers (CNFs) without any subsequent physical or chemical activation. The concept developed here avoids unnecessary and complex extra activation steps when fabricating CNFs which ultimately lead to lower char yields and uncontrollable pore sizes. The ability of COOH in P(AN-co-IA) to act as an in situ porogen by releasing CO2 during carbonization was verified by simultaneous thermogravimetric analysis-mass spectrometry compared to polyacrylonitrile (PAN). The specific surface area of PAN CNFs (27 m2 g−1) dramatically increases to 1427 m2 g−1 upon addition of ∼8 wt% IA without any ex situ activation. Furthermore, we confirmed that the porosity could be tuned by changing the IA content. The best electrochemical performance was obtained from the copolymer containing ∼8 wt% of IA, which gives a maximum specific capacitance of ∼93 F g−1 at a scan rate of 10 mV s−1 and energy density of ∼46 Wh kg−1 at 1 A g−1 without any subsequent physical or chemical activation. [ABSTRACT FROM AUTHOR]

Lignin was blended with polyacrylonitrile (PAN) in different ratios and fabricated into carbon nanofiber electrodes by electrospinning followed by thermal stabilization, carbonization and subsequent activation by CO2 of the carbonized mats. These carbon fiber electrodes exhibit high surface area, high mesoporosity, high graphitic content and high electrical conductivity. Activated carbon nanofiber mats derived from PAN:Lignin 70:30 blends display a surface area of 2370 m2 g−1 with 0.635 cm3 g−1 mesopore volume. These results are due to the selective partial removal of carbonized lignin during the activation step. Coin cell supercapacitors employing these electrodes exhibit 128 Fg−1 specific capacitance, 59 Wh kg−1 energy density and a 15 kW kg−1 power density when operated at 3.5 V using an ionic liquid electrolyte. Since lignin is an inexpensive, abundant, and green polymer, incorporating it into carbon blends enhances the scalability of such materials in energy storage applications. [ABSTRACT FROM AUTHOR]

Flexible, free standing and binder-free electrodes were fabricated by electrospinning from a series of lignin: polyvinyl alcohol (PVA) polymer blends, followed by heat treatment. PVA has the dual function of facilitating the electrospinning of lignin and acting as a sacrificial polymer. Upon stabilization, carbonization and CO2 activation, carbon nanofibers (ACNF) derived from the lignin:PVA 80:20 blend displayed a high surface area of 2170 m2 g−1 and a mesopore volume of 0.365 cm3 g−1. ACNFs derived from all the compositions show high degrees of graphitization based on Raman analysis. Pyr14TFSI ionic liquid (IL), modified by mixing with propylene carbonate and ethylene carbonate to reduce the viscosity and increase the ionic conductivity, was used as a high-performance electrolyte. The resulting IL mixture exhibited a four-fold increase in ionic conductivity compared to the neat IL Coin cell supercapacitors using electrodes derived from lignin:PVA 80:20 blends and this electrolyte displayed 87 F g−1 specific capacitance and 38 Wh kg−1 energy density which is the highest reported energy density for lignin:PVA blends to date. [ABSTRACT FROM AUTHOR]

Carbon nanofibers (CNFs) are promising electrode materials for electrochemical double layer capacitors due to their high porosity and electrical conductivity. CNFs were prepared by electrospinning and subsequent thermal treatment of a new precursor polymer, 6FDA-durene, without the addition of pore generating agents. The conversion of precursor nanofibers into CNFs was confirmed using Raman spectroscopy. CNFs were activated and annealed, and nitrogen adsorption/desorption measurements were conducted to determine surface area and porosity. These activated/annealed CNFs were used as binderless electrodes in coin cells with an ionic liquid electrolyte. The devices displayed a specific capacitance of 128 F g−1, an energy density of 63.4 Wh kg−1 (at 1 A g−1), and a power density of 11.0 KW kg−1 (at 7 A g−1). [ABSTRACT FROM AUTHOR]

Porous carbon nanofibers were prepared by electrospinning blend solutions of polybenzimidazole/poly-L-lactic acid (PBI/PLLA) and carbonization. During thermal treatment, PLLA was decomposed, resulting in the creation of pores in the carbon nanofibers. From SEM images, it is shown that carbon nanofibers had diameters in the range of 100–200 nm. The conversion of PBI to carbon was confirmed by Raman spectroscopy, and the surface area and pore volume of carbon nanofibers were determined using nitrogen adsorption/desorption analyses. To investigate electrochemical performances, coin-type cells were assembled using free-standing carbon nanofiber electrodes and ionic liquid electrolyte. cyclic voltammetry studies show that the PBI/PLLA-derived porous carbon nanofiber electrodes have higher capacitance due to lower electrochemical impedance compared to carbon nanofiber electrode from PBI only. These porous carbon nanofibers were activated using ammonia for further porosity improvement and annealed to remove the surface functional groups to better match the polarity of electrode and electrolyte. Ragone plots, correlating energy density with power density calculated from galvanostatic charge–discharge curves, reveal that activation/annealing further improves energy and power densities. [ABSTRACT FROM AUTHOR]